Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

Starlight Cardiovascular Lifeline Ductus Arteriosus Stent IDE Study

NCT07114718 · View on ClinicalTrials.gov ↗

Study Summary

Starlight Cardiovascular, Inc. is sponsoring a prospective, multi-center, study to evaluate safety and effectiveness of the Lifeline Ductus Arteriosus Stent System. The study device is a stent that is designed to maintain patency of the Ductus Arteriosus for children who need blood flow through that part of the heart.

Interventions

  • DEVICE Ductus Arteriosus Stent

Study Locations (7)

California

  • UCLA Mattel Children's — Los Angeles
  • Leland Stanford Junior University — Stanford

Ohio

  • Cincinnati Children's Hospital Medical Center — Cincinnati
  • Nationwide Children's Hospital — Columbus

Colorado

  • Children's Hospital Colorado — Aurora

Massachusetts

  • Boston Children's Hospital — Boston

Washington

  • Seattle Children's Hospital — Seattle

Trial Details

FieldValue
Enrollment Target 35 participants
Start Date 2025-12-03
Est. Completion 2028-04
Phase NA

Sponsor

Starlight Cardiovascular

1 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07114718

The ClinicalTrials.gov registry entry for NCT07114718 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 35 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Starlight Cardiovascular, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Congenital Heart Disease appearing as the primary indexed condition, and to 1 intervention — of which Ductus Arteriosus Stent is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07114718 reports 7 study locations spanning 5 distinct geographic areas — top geographies include California, Ohio, Colorado. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07114718 about?

NCT07114718 is a clinical study titled "Starlight Cardiovascular Lifeline Ductus Arteriosus Stent IDE Study". Starlight Cardiovascular, Inc. is sponsoring a prospective, multi-center, study to evaluate safety and effectiveness of the Lifeline Ductus Arteriosus Stent System. The study device is a stent that is designed to maintain patency of the Ductus Arteriosus for children who need blood flow through that...

What is the current status of trial NCT07114718?

This trial is currently recruiting. It is a NA study. The enrollment target is 35 participants. The study started on 2025-12-03. Estimated completion is 2028-04.

What conditions does trial NCT07114718 study?

This clinical trial studies the following conditions: Congenital Heart Disease, Congenital Heart Disease (CHD). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07114718?

The interventions under investigation include: Ductus Arteriosus Stent (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07114718?

This trial is sponsored by Starlight Cardiovascular, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07114718 being conducted?

This trial has 7 study locations across California, Colorado, Massachusetts, Ohio, Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial